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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.
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ManufacturerBrand NameDate Report Received
NUVASIVE INC SIMPLIFY CERVICAL ARTIFICIAL DISC 11/01/2023
NUVASIVE INC SIMPLIFY CERVICAL ARTIFICIAL DISC 11/01/2023
NUVASIVE INC SIMPLIFY CERVICAL ARTIFICIAL DISC 10/30/2023
MEDTRONIC SOFAMOR DANEK USA, INC PRESTIGE DISC 10/26/2023
NUVASIVE INC SIMPLIFY CERVICAL ARTIFICIAL DISC 10/24/2023
LDR MEDICAL MOBI-C IMPLANT "M" STANDARD, UNKNOWN SIZ 10/19/2023
MEDOS INTERNATIONAL SàRL CH UNKNOWN ARTIFICIAL DISC REPLACEMENT 10/10/2023
NUVASIVE INC SIMPLIFY CERVICAL ARTIFICIAL DISC 10/03/2023
NUVASIVE INC SIMPLIFY CERVICAL ARTIFICIAL DISC 10/03/2023
LDR MEDICAL MOBI-C IMPLANT "M" STANDARD 15X15 H5 US 08/15/2023
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